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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142894insertion1nstd232human GRCh37.p13 chr2: 86,997,251-86,997,251 , GRCh38.p12 chr2: 86,770,128-86,770,128 RMND5A
    nsv7045520inversion1nstd229human GRCh38 chr2: 86,706,307-86,887,942 , GRCh37.p13 chr2: 86,933,430-87,115,065 CD8B, ANAPC1P1, 4 more genes
    nsv6686702copy number variation1nstd229human GRCh38 chr2: 86,773,731-86,773,805 , GRCh37.p13 chr2: 87,000,854-87,000,928 RMND5A
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628358copy number variation1nstd224human GRCh37 chr2: 86,969,771-87,171,150 , GRCh38.p12 chr2: 86,742,648-86,944,027 CD8A, CD8B, 6 more genes
    nsv6628159copy number variation1nstd224human GRCh37 chr2: 86,974,049-87,123,114 , GRCh38.p12 chr2: 86,746,926-86,895,991 CD8B, RMND5A, 3 more genes
    nsv6550678inversion1nstd223human GRCh38 chr2: 86,766,400-86,767,342 , GRCh37.p13 chr2: 86,993,523-86,994,465 RMND5A
    nsv6345881copy number variation1nstd223human GRCh38 chr2: 86,743,818-86,744,058 , GRCh37.p13 chr2: 86,970,941-86,971,181 RMND5A
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 LOC105374836, LOC105374833, 93 more genes
    nsv6311603copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,067,267-87,017,948 , GRCh38.p12 chr2: 85,840,144-86,790,825 CHMP3-AS1, RNF103-CHMP3, 16 more genes
    nsv6140232copy number variation1nstd206human GRCh38 chr2: 86,722,850-86,729,154 , GRCh37.p13 chr2: 86,949,973-86,956,277 RMND5A
    nsv5990189copy number variation1nstd212human GRCh38 chr2: 86,762,667-86,762,719 , GRCh37.p13 chr2: 86,989,790-86,989,842 RMND5A
    nsv5833476copy number variation2nstd209human GRCh38 chr2: 86,719,673-86,722,579 , GRCh37.p13 chr2: 86,946,796-86,949,702 RNF103-CHMP3, RMND5A
    nsv5725738mobile element insertion1nstd211human GRCh38 chr2: 86,764,811-86,764,811 , GRCh37.p13 chr2: 86,991,934-86,991,934 RMND5A
    nsv5584043copy number variation1nstd207human GRCh38 chr2: 86,743,083-86,743,219 , GRCh37.p13 chr2: 86,970,206-86,970,342 RMND5A
    nsv5569255copy number variation1nstd207human GRCh38 chr2: 86,743,083-86,744,006 , GRCh37.p13 chr2: 86,970,206-86,971,129 RMND5A
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5540186insertion1nstd206human GRCh38 chr2: 86,762,071-86,762,100 , GRCh37.p13 chr2: 86,989,194-86,989,223 RMND5A
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